rs1057519606

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs1057519606(C;C)

Make rs1057519606(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

18159349

Gene

MYO15A

is a	snp
is	mentioned by
dbSNP	rs1057519606
dbSNP (classic)	rs1057519606
ClinGen	rs1057519606
ebi	rs1057519606
HLI	rs1057519606
Exac	rs1057519606
Gnomad	rs1057519606
Varsome	rs1057519606
LitVar	rs1057519606
Map	rs1057519606
PheGenI	rs1057519606
Biobank	rs1057519606
1000 genomes	rs1057519606
hgdp	rs1057519606
ensembl	rs1057519606
geneview	rs1057519606
scholar	rs1057519606
google	rs1057519606
pharmgkb	rs1057519606
gwascentral	rs1057519606
openSNP	rs1057519606
23andMe	rs1057519606
SNPshot	rs1057519606
SNPdbe	rs1057519606
MSV3d	rs1057519606
GWAS Ctlg	rs1057519606

Max Magnitude

0

ClinVar
Risk	rs1057519606(C;C)
Alt	rs1057519606(C;C)
Reference	Rs1057519606(T;T)
Significance	Pathogenic
Disease	Deafness
Variation	info
Gene	MYO15A
CLNDBN	Deafness, autosomal recessive 3
Reversed	0
HGVS	NC_000017.10:g.18062663T>C
CLNSRC
CLNACC	RCV000417166.1,